ライフサイエンスコーパス: cannot

1 ay have an adaptive advantage over those who cannot.

2 hronize their movements in ways that novices cannot.

3 while changes in predator-prey interactions cannot.

4 emaining absorption surface of the intestine cannot absorb enough macronutrients, micronutrients, and

5 jacent motif (PAM) requirements, CRISPR/Cas9 cannot access many genetic loci.

6 GxE genome-wide are nascent and, as we show, cannot accommodate general environment variables, modest

7 However, their fixed dimensions cannot accommodate rapid tissue growth(4,5) and may impa

8 times for end-of-epidemic declarations that cannot accommodate these variations.

9 This model cannot account for interactions of edges with one anothe

10 Although photoevaporation rates cannot account for the mass loss required to reduce a Ju

11 Existing computational methods cannot accurately reconstruct activities of individual c

12 llows for rapid staining, but these sections cannot accurately represent three-dimensional structures

13 bserve that all the state-of-the-art methods cannot achieve an ideal accuracy for overlap detection (

14 but its diagnostic accuracy is limited as it cannot adequately distinguish between true tumor progres

15 The time to act is now and we cannot afford to ignore the new solutions that GM provid

16 dies, where optimal pre-analytical condition cannot always be guarantee.

17 putational cost, existing region-based tests cannot analyze hundreds of thousands of samples while ac

18 nic degeneracy or pseudodegeneracy, but they cannot be a priory fully excluded for any system.

19 Neoproterozoic Snowball Earth and therefore cannot be a product of glacial erosion.

20 ue to sp(2) carbon-conjugated frameworks and cannot be accessible by imine-linked frameworks, amorpho

21 3D perovskite AMX(3) structure because they cannot be accommodated in the cubo-octhedral cage (do no

22 ing the transition toward circularity, which cannot be achieved by technology improvements alone-the

23 These attributes often cannot be achieved by traditional molecular sensors i.e.

24 Such cannot be achieved by utilizing capsid sequence data alo

25 x biological regulatory mechanisms when this cannot be achieved solely through experimental approache

26 luorescence imaging of kidney cancers, which cannot be achieved with hepatobiliary- and glomerular-cl

27 antagonizing platelet integrin alphaIIbbeta3 cannot be achieved without compromising hemostasis, thus

28 ing residues 1-4 are functional Rubiscos but cannot be activated.

29 This question cannot be answered by simply recording from multiple bra

30 Importantly, most methods cannot be applied to either GWAS/eQTL summary statistics

31 the fluorescent particles can diffuse, they cannot be applied to situations in which this region is

32 here liquid chromatography-MS-based analyses cannot be applied.

33 of choice when dealing with matrix data that cannot be arranged into a trilinear three-way array, tha

34 low abundances of amino acids in Tagish Lake cannot be ascribed to fluid chemistry.

35 also suggests that ATP and NAD(P)H balancing cannot be assessed in isolation from each other, or even

36 surgical intervention's impact on mortality cannot be assessed in this study, as it would need to be

37 Treatment efficacy cannot be assessed with this measure during clinical tri

38 potential periprosthetic shoulder infection cannot be assumed.

39 tems also exhibit specific reactivities that cannot be attained with regular substrates.

40 ent anti-biofilm activity of Bald's eyesalve cannot be attributed to a single ingredient and requires

41 ress, however successful fragile site repair cannot be calculated using existing techniques.

42 Treg) during coculture assays, features that cannot be captured by using surrogate cell lines or anim

43 In humans, clinical manifestation of tics cannot be captured via functional imaging due to motion

44 Organic liquids, however, cannot be charged effectively by existing methods due to

45 othalamic tract, and other deep brain nuclei cannot be clearly identified.

46 Partial flow recovery with forest age cannot be commonly expected, however, and forestation pr

47 , sIPV products from different manufacturers cannot be compared, and the relationship between antigen

48 AC has an essential and unique function that cannot be compensated by other HDAC complexes.

49 Residual confounding by comorbid conditions cannot be completely excluded.

50 liferation, and note that these observations cannot be conducted within previous continuum models of

51 suming and more often is only indicative and cannot be considered confirmative as it is susceptible t

52 Accordingly, patients with burn injury cannot be considered recovered when the wounds have heal

53 icates that the development of mental health cannot be considered without consideration of children i

54 The filaments inside the bundle cannot be continuously actuated, nor can they easily unb

55 that when population structure is recent, it cannot be corrected using principal components of common

56 Such posttreatment confounding cannot be dealt with using standard methods (e.g., gener

57 eans that a symbol must be taken as such and cannot be decomposed into signal and noise.

58 specific adverse effects of ROS1 inhibition cannot be deconvoluted from the toxicity profiles of the

59 This fact suggests that RFs of SDs cannot be defined as homogeneous sensory zone driven by

60 such as remdesivir and reconvalescent serum cannot be delivered orally(2,3), making them poorly suit

61 cancer screening, the number of cancers that cannot be detected with mammography is substantial, espe

62 ctions are difficult to analyze because they cannot be determined by comparing the energies of compet

63 pecies transmission and the drivers for this cannot be determined from this study.

64 harms of screening for cognitive impairment cannot be determined.

65 that the biodegradation performance in soils cannot be directly assessed by measuring the expression

66 In contrast, PopZ and SpmX cannot be directly identified in CET.

67 hnical limitation of estimating g(m) , which cannot be directly measured, and (iv) how g(m) responds

68 le costs on society; however, their benefits cannot be directly observed and are currently understood

69 on structure and transcriptional states that cannot be discerned from bulk measurements, establishing

70 tributions from homologous antenna complexes cannot be disentangled.

71 a 1:1 protein-lipid complex, where the lipid cannot be displaced by detergent from the highly protect

72 toxin A gene (sea) causes food poisoning and cannot be distinguished from non-pathogenic strains by t

73 ble elements from which reliable conclusions cannot be drawn, and therefore has made the decision to

74 f cryptic lineages within the upwelling zone cannot be easily accounted for by environmental heteroge

75 e inherent property of a given material that cannot be easily changed at will.

76 probes are limited in scope, though, as they cannot be easily distinguished in biological environment

77 changes at local scale are often complex and cannot be easily generalized.

78 Since SOC content of soils cannot be easily measured, a key barrier to implementing

79 ls based on their migratory characteristics, cannot be easily performed.

80 We show that the striped fibrillar pattern cannot be easily predicted from the interactions between

81 ression system or show unusual features that cannot be easily programmed in living organisms.

82 nate human senses, the complexity perception cannot be easily quantified.

83 This causes problems when the biosensor cannot be easily replaced (e.g., implanted electronics).

84 uence complexity (TTAGGG)n of telomeres that cannot be easily resolved through sequencing.

85 The reaction is truly three-component and cannot be effectively performed stepwise.

86 Since phosphate cannot be efficiently removed by dialysis, the resulting

87 : 2.93, 1.79-4.79; confounding by indication cannot be excluded).

88 Given a small effect on CHD cannot be excluded, further investigation with stronger

89 However, traditional chemical inhibitors cannot be experimentally applied with spatiotemporal pre

90 g learning and memory; however, this process cannot be explained by a simple linear trajectory of tra

91 ifts observed in several FLE conditions that cannot be explained by alternative (temporal) models of

92 The increase seen across birth cohorts cannot be explained by changes in occupation or levels o

93 duced iodine emissions from natural seawater cannot be explained by chemical losses of I(2) or hypoio

94 s a lower genotype-derived heritability that cannot be explained by inclusion of milder cases and a h

95 2) the dapagliflozin-induced increase in EGP cannot be explained by the increase in plasma glucagon o

96 Importantly, the latter cannot be explained by theta power changes, head movemen

97 deep low-stability layer in the polar region cannot be explained by vertical convection in the middle

98 ovir toxicity in patients taking ART for HIV cannot be explained solely on the basis of off-target in

99 ral rearrangement in the process XS -> XS(-) cannot be explained using the values of the electron det

100 These values cannot be explained with classical models for optical ou

101 ysical properties which are averaged out and cannot be exploited in disordered systems.

102 differentiated for effective sensing, which cannot be fulfilled by common PDs with a broadband respo

103 As yet, this multi-length-scale complexity cannot be fully captured by atomistic simulations, and t

104 ted that annual phytoplankton biomass cycles cannot be fully understood from environmental properties

105 ctions and network architectures exists, but cannot be fully understood without attention to the envi

106 al profile was dependent on the cultivar and cannot be generalised.

107 mary pseudotumor cerebri, in which the cause cannot be identified (also known as idiopathic intracran

108 racteristics with mammalian enteric glia but cannot be identified by the expression of canonical glia

109 ss weak magnetic remanence (Fe(3) O(4) ), or cannot be implemented in nanofabrication schemes (NdFeB)

110 challenge for cells is that these objectives cannot be independently optimized, and maximizing one of

111 heir conditional informativeness for disease cannot be inferred from their accuracy in predicting reg

112 I antimicrobial susceptibility testing (AST) cannot be interpreted using recognized standards.

113 ti-spin nanoscale devices, because the field cannot be localized or screened.

114 Unfortunately, many control measures cannot be maintained indefinitely, and the results of ce

115 The true population LD cannot be measured directly and instead can only be infe

116 xplain phenotypes of genetic diseases, which cannot be obtained by transcript information alone.

117 d variance, scores, and other results, which cannot be obtained in the conventional cross-validation.

118 urface response (i.e., heterogeneity), which cannot be obtained solely by an electrochemical means.

119 ss spectrometry for accurate diagnosis of MN cannot be overemphasized.

120 ods for SCD are time-consuming, complex, and cannot be performed at point-of-care (POC) and home sett

121 gh the generation of mice in which eIF2alpha cannot be phosphorylated specifically in Schwann cells.

122 Hydroxychloroquine exposure is low and cannot be predicted by other populations.

123 the success or failure of a given structure cannot be predicted by quality metrics such as resolutio

124 Since the pathway of resistance cannot be predicted, combination therapies may address t

125 the specific metal used by any family member cannot be predicted.

126 ks are not stabilized, and new origin firing cannot be prevented, leading to the accumulation of DNA

127 dels, we demonstrate that these observations cannot be produced by previously proposed horizontal ext

128 fore a full range of template concentrations cannot be quantified accurately with these methods alone

129 es, yet animals eventually reject tumors and cannot be raised at 37 degrees C.

130 hydrogels with a desirable network structure cannot be readily achieved using conventional polymeriza

131 g of complex genomic regulation in vivo that cannot be readily investigated through standard methodol

132 ow is well suited to biological samples that cannot be readily isotope labeled, including plants, mam

133 ents after ischaemic stroke, and thus S44819 cannot be recommended for stroke therapy.

134 days of storage to be used in a DMEK surgery cannot be recommended.

135 difficulties incorporating binding data, and cannot be reduced or connected to simpler forms.

136 those claiming that one's scientific impact cannot be reduced to a single number.

137 not ideal because often the null hypothesis cannot be rejected simply due to limited statistical pow

138 s of gasteroid forms are highly unlikely but cannot be rejected.

139 Second, because ADE of disease cannot be reliably predicted after either vaccination or

140 to inappropriate post-harvest processing and cannot be removed in the subsequent chocolate-manufactur

141 ng that this property is highly variable and cannot be represented by a single value based on the AO-

142 female lethality of DH6 is 100% dominant and cannot be repressed by maternal tetracycline.

143 c behavior observed in synaptic transmission cannot be reproduced in a standard kinetic model without

144 linical experiments are giving results which cannot be reproduced.

145 Ubiquitous pathological triggers cannot be responsible for the selective neuron loss.

146 sclose biological discoveries that otherwise cannot be revealed by existing approaches.

147 ls measured in the general population, risks cannot be ruled out due to the potential for population

148 ity of neuroinvasiveness of the virus, which cannot be ruled out given the expression of low levels o

149 Although unmeasured confounding cannot be ruled out, when analyzed by time periods, or a

150 uire field experts to create them, and often cannot be shared outside the lab due to medical regulati

151 Thus, biodiversity changes cannot be solely viewed as a response to human influence

152 d injury at the cellular and molecular level cannot be studied in vivo.

153 ange and human response and argue that these cannot be successfully addressed without an understandin

154 However, a full lockdown cannot be sustained for a prolonged period.

155 is do not occur on the Mexican Pacific coast cannot be sustained.

156 chitin into two aromatic NCCs that currently cannot be synthesized from chitin via any chemical proce

157 e access to the properties of compounds that cannot be synthesized in single-phase form, sparing cost

158 -50% or less in many cohorts, a good ranking cannot be taken to imply that the gene or disease at ran

159 own or inaccessible activity profiles and so cannot be targeted by such strategies.

160 This assumption cannot be tested directly, but it can be falsified.

161 lly polar, it is heavily disordered and this cannot be the sole reason for the ferroelectricity.

162 replicate in these mosquitoes and therefore cannot be transmitted to people even in the unlikely eve

163 ntions to mitigate them even in patients who cannot be transplanted.

164 mena that can be surprisingly rich and often cannot be understood by studying only the individual con

165 r osmolarity measured with TearLab osmometer cannot be used as a key indicator of DED.

166 an quantify corneal elasticity ex vivo, they cannot be used clinically.

167 ality assumption are readily available, they cannot be used directly because the included studies hav

168 ltra as a single diagnostic test for TBM; it cannot be used to "rule out" TBM.

169 Proliferation rates alone cannot be used to achieve cancer specificity.

170 Consequently, D-dimer cannot be used to exclude DVT without an assessment of p

171 ber of core single nucleotide variants alone cannot be used to infer cross-transmission in M. abscess

172 al intensity, such as those for well plates, cannot be used to quantify signal from most of these dev

173 mice and all existing humanized mouse models cannot be used to test the efficacy of vaccines expressi

174 re inefficient because lower-quality samples cannot be used, and they assume individuals are identifi

175 tings where existing experimental strategies cannot be used.

176 Coronary microcirculation cannot be visualized in vivo in humans, and functional i

177 nitive or reward-related impairments, yet it cannot be wholly related to one or the other process and

178 emperatures for growth and processing, which cannot be withstood by the substrate underneath.

179 g hyperactive MYC transcription factors that cannot bind JAZ repressors.

180 rupt editing in vitro, suggesting that PPR65 cannot bind modified bases due to differences in the str

181 While L11 protein cannot bind to the GAC until the RNA has adopted its ter

182 We argue that statistical measures alone cannot capture all structural aspects of LCRs and recomm

183 method for analyzing rational process models cannot capture an important constraint on resource alloc

184 y are usually very successful but inherently cannot capture the quantum-optical nature of the process

185 ch is composed of a grating and line sensor, cannot capture the spectral behavior from noise to stabl

186 ture whereas traditional FSSs are static and cannot change their performance.

187 ovo emergence of resistance even though they cannot clear already-large resistant populations.

188 Legumain cannot cleave after glycosylated Asn residues, which ena

189 Bovine derived chymosin in rennet cannot coagulate camel milk (CAM).

190 When we face ambiguous images, the brain cannot commit to a single percept; instead, it switches

191 We show that NLGN4Y cannot compensate for the functional deficits observed i

192 rly studies suggested that Fe(III) complexes cannot compete with Gd(III) complexes as T(1) MRI contra

193 y, AID(S38A/S38A)UNG(-/-) mouse B cells also cannot complete CSR or affinity maturation despite accum

194 Although our results cannot conclude physical fitness is related to white mat

195 ks the ability to initiate transcription and cannot consistently transcribe through long DNA sequence

196 Furthermore, this mutant cannot correct alterations in both Syt1 expression and t

197 otential value of refined tools of this sort cannot currently be made because such an assessment woul

198 ersistently even if its cortical contraction cannot deform a near-rigid ECM, but then the contraction

199 le sulfate to oxidize the sub-arc mantle and cannot deliver (34)S-enriched sulfur to produce the posi

200 Cohort studies cannot determine causality, and current disease severity

201 unts in people's vaccine decision-making, it cannot determine whether different degrees of severity i

202 We also cannot determine whether observed changes in purchases a

203 tractant gradients between a source and sink cannot direct cells over such ranges.

204 These cohort-based approaches cannot directly identify individual pathogenic noncoding

205 us on prioritization of candidate genes, and cannot directly infer the specific functional effects of

206 hermore, we show that predictive information cannot distinguish between organisms that are adapted to

207 on about leukaemia biology and prognosis, it cannot distinguish which mutations occur in the same clo

208 its interactions, but most in vitro studies cannot duplicate the unique spatial arrangement of cMyBP

209 capturing a subset of cleansing effects, but cannot easily handle cleansing effects in non-moral, non

210 , required for NMR excitation and detection, cannot easily penetrate the battery casing due to the sk

211 bit structural and molecular alterations and cannot effectively compensate for fluid extravasation an

212 Therefore, these methods cannot effectively correct all misalignments.

213 ficult because available therapeutic regimen cannot effectively kill and eliminate ERPC cells.

214 lysogenic), type I CRISPR-Cas immune systems cannot eliminate the phages from the bacterial populatio

215 rphological measurements of the root systems cannot entirely explain variations in citrate-enhanced u

216 Although we cannot exclude other differences, and in particular alte

217 iring more anti-VEGF injections; however, we cannot exclude that the RNFL thinning may be secondary t

218 g extends classical computing means that one cannot expect arbitrary simulations to be sped up by a q

219 vealed that carrier-mediated transport alone cannot explain the experimentally determined auxin distr

220 ulk tissue eQTLs, although disease relevant, cannot explain the majority of disease heritability.

221 However, this hypothesis cannot explain the multi-Myr lag between the delta(13)C

222 Two-population models cannot explain the results.

223 at belowground morphological diversity alone cannot explain this rate increase.

224 Here, we show that TMC1/2 cannot form mechanotransduction channels in cochlear hai

225 l prefrontal cortex, but not in animals that cannot form new myelin.

226 Consequently, one cannot formally examine whether hospitals that have poor

227 egeneration expected at genomic regions that cannot freely recombine.

228 purely bottom-up statistical learning alone cannot fully account for the ability to create abstract

229 om effect for a genetic relationship matrix, cannot fully account for the fine-scale geographical con

230 th two stimulus categories, but such designs cannot fully capture the limitations inherent in natural

231 rent methods for analyzing diploid Hi-C data cannot fully distinguish between homologous chromosomes.

232 groups also harbor ancestry from sources we cannot fully model with the available data, highlighting

233 in well myelinated mice in which glial cells cannot fully support axons metabolically.

234 Hence, -10 elements cannot function in isolation.

235 reports, we find that protonation reactions cannot generally be classified as either charge- or fron

236 ay, as activating autophagy when the pathway cannot go to completion (e.g., when lysosomal degradatio

237 We cannot, however, evaluate the efficacy of treatments wit

238 GWAS cannot identify functional SNPs (fSNP) from disease-asso

239 vivo studies, may reduce the TTI further, it cannot increase it.

240 ho sees the responses to random inputs-still cannot infer responses to new inputs?

241 s the AID phosphorylation mutant, AID(S38A), cannot interact with APE1, a BER protein.

242 omyces cerevisiae strains in which MutLgamma cannot interact with PCNA present defects in forming cro

243 n of rnhA to encode an RNase HI variant that cannot interact with SSB but that maintains enzymatic ac

244 y care, and the current hepatology workforce cannot meet the demand of patients with liver disease na

245 Moreover, evidence suggests infections cannot neatly be separated into the dichotomy of droplet

246 gest that predictable molecular organization cannot normally be achieved using these embraces, which

247 stable in (CAG)n = even, but such situation cannot occur in (CAG)n = odd, where the hairpin is "frus

248 Meanwhile, MT-SCCALR cannot only select relevant SNPs and imaging QTs for eac

249 Thus, c-di-GMP cannot only stabilize domain interactions, but also enga

250 improve quality and access for patients who cannot, or choose not to, receive their care at high-vol

251 ETs are in an inactive conformation and thus cannot participate in further catalytic events.

252 mining motion in the environment, but humans cannot perform this task without error.

253 proliferative advantage, below which mutants cannot persist.

254 riables do not correlate which means that we cannot predict patient survival solely based on the init

255 substantial overpotential is applied, and it cannot produce H(2).

256 S biosynthesis and that an HH103 rkpM mutant cannot produce KPS and displays an altered LPS structure

257 Similarly, an ept1Delta/Delta mutant, which cannot produce PE by the Kennedy pathway, exhibits decre

258 means that the groups enter areas where they cannot profit from local knowledge.

259 e mostly based on physical examinations that cannot provide information about the exact location of c

260 However, existing empirical methods often cannot provide key genetic and functional details requir

261 oint-of-care analysis or home monitoring and cannot provide real-time readouts.

262 ommon and lethal syndrome in which the heart cannot pump blood to adequately meet bodily demands, res

263 However, we discovered that bursting alone cannot quantitatively recapitulate the formation of the

264 Here we show that static abiotic dissolution cannot rationalize this result, whereas two dynamic abio

265 Based on the present findings, we cannot recommend continuous intranasal oxytocin treatmen

266 ally reparable pores generated by LEEFT that cannot recover in the subsequent ozonation and the great

267 , the existing peak deconvolution algorithms cannot recover the accurate expression level of genes in

268 The result cannot reflect spurious selection of out-of-system areas

269 The tracer cannot reliably differentiate non-Alzheimer tauopathies

270 t electrophysiological or optical techniques cannot reliably perform simultaneous intracellular recor

271 imCells can be used as a safe agent (as they cannot replicate) for bacterial therapy.

272 While one-sided loop extrusion cannot reproduce these phenomena, variants can recapitul

273 However, ectopic DPP cannot rescue the anterior fate formation, suggesting ad

274 lay in neuronal birth, suggesting that Ascl1 cannot rescue the loss of Neurog2 and that these proneur

275 orientations in the phospholipid bilayer but cannot resolve the actual distribution of molecules embe

276 Conventional analytical techniques cannot resolve the distribution of excipients and drugs

277 Current theories cannot resolve this apparent contradiction.

278 However, they cannot reveal key structural information, e.g., lectin's

279 which an organism is exposed, these sensors cannot reveal the presence and extent of internal tissue

280 ext of systemic LCMV or VV infection, but we cannot rule out the possibility that the generation of T

281 ed original science, conceptual replications cannot serve as the field's self-correction mechanism.

282 However, conventional patterning methods cannot simultaneously meet the stringent requirements of

283 Large organic A cations cannot stabilize the 3D perovskite AMX(3) structure beca

284 In the latter, an individual cannot stop using a drug despite major negative conseque

285 regimes in which population structure alone cannot support coexistence, suggesting the need for othe

286 01D/S241D, a phosphorylation-mimicry mutant, cannot suppress VEGFA expression to support normal vascu

287 han 3.5-6%; and iv) the total sterol content cannot surpass 2400 mg/kg.

288 he spread of resistance, but small companies cannot survive on revenues that do not cover operational

289 enic genes to other organisms, and that they cannot survive to propagate in unintended environments,

290 These include compounds that pups cannot synthesise themselves, such as pyridoxine/vitamin

291 Because Nitrobacter spp. cannot synthesize cobalamin, we postulate that they acqu

292 E. chaffeensis cannot synthesize phosphatidylcholine or cholesterol but

293 data to ASD; however, this previous approach cannot take into account for prior biological knowledge.

294 alkylation with mesitylene, a reaction that cannot take place in the zeolite micropores, is observed

295 materials, such as conventional metal films, cannot tolerate.

296 This indicates that some plankton species cannot track optimal temperatures on a global scale as a

297 nce to a near-scientific certainty that they cannot transfer their transgenic genes to other organism

298 stranded (ds) complex that does not fit and cannot traverse this nanopore.

299 ve analysis of alpha7 with its homologs that cannot trigger channel opening has not been made so far.

300 ltifactorial pathophysiological process that cannot yet be recapitulated in a single in vitro model.